Boris Pasche

10.0k total citations · 2 hit papers
122 papers, 5.9k citations indexed

About

Boris Pasche is a scholar working on Oncology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Boris Pasche has authored 122 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Oncology, 57 papers in Molecular Biology and 27 papers in Pathology and Forensic Medicine. Recurrent topics in Boris Pasche's work include TGF-β signaling in diseases (30 papers), Genetic factors in colorectal cancer (25 papers) and Pancreatic and Hepatic Oncology Research (22 papers). Boris Pasche is often cited by papers focused on TGF-β signaling in diseases (30 papers), Genetic factors in colorectal cancer (25 papers) and Pancreatic and Hepatic Oncology Research (22 papers). Boris Pasche collaborates with scholars based in United States, China and Switzerland. Boris Pasche's co-authors include John Varga, Yanfei Xu, Virginia Kaklamani, Loren S. Michel, Michael J. Pennison, Naresh Bellam, Paul J. Grippo, William L. Gerald, Vundavalli V. Murty and Robert Benezra and has published in prestigious journals such as Nature, Science and JAMA.

In The Last Decade

Boris Pasche

116 papers receiving 5.8k citations

Hit Papers

MAD2 haplo-insufficiency causes premature anaphase and ch... 2001 2026 2009 2017 2001 2014 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Boris Pasche United States 40 3.0k 2.1k 1.2k 963 793 122 5.9k
Mark A. Watson United States 48 3.4k 1.1× 1.9k 0.9× 1.7k 1.4× 794 0.8× 1.4k 1.8× 129 7.2k
Giuseppe Viglietto Italy 48 5.4k 1.8× 2.3k 1.1× 1.6k 1.3× 591 0.6× 803 1.0× 150 8.2k
Toshiyuki Ishiwata Japan 47 3.6k 1.2× 2.5k 1.2× 1.4k 1.2× 387 0.4× 586 0.7× 215 6.4k
Vladimir Lazar France 46 4.1k 1.3× 2.1k 1.0× 2.1k 1.7× 607 0.6× 954 1.2× 133 7.4k
Dilip D. Giri United States 37 3.0k 1.0× 2.9k 1.4× 2.4k 2.0× 1.1k 1.1× 712 0.9× 94 7.0k
Colin A. Purdie United Kingdom 35 2.8k 0.9× 3.3k 1.6× 1.8k 1.5× 932 1.0× 552 0.7× 92 6.5k
Kwok Wah Chan Hong Kong 46 3.2k 1.0× 2.5k 1.2× 1.7k 1.4× 687 0.7× 945 1.2× 162 8.0k
Fei Huang China 35 3.2k 1.1× 1.7k 0.8× 1.5k 1.2× 575 0.6× 711 0.9× 190 6.5k
Carl Morrison United States 45 4.2k 1.4× 2.3k 1.1× 2.4k 2.0× 922 1.0× 1.3k 1.6× 185 8.1k
Jacob Pe’er Israel 39 3.6k 1.2× 1.8k 0.8× 1.2k 1.0× 336 0.3× 658 0.8× 149 7.7k

Countries citing papers authored by Boris Pasche

Since Specialization
Citations

This map shows the geographic impact of Boris Pasche's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Boris Pasche with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Boris Pasche more than expected).

Fields of papers citing papers by Boris Pasche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Boris Pasche. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Boris Pasche. The network helps show where Boris Pasche may publish in the future.

Co-authorship network of co-authors of Boris Pasche

This figure shows the co-authorship network connecting the top 25 collaborators of Boris Pasche. A scholar is included among the top collaborators of Boris Pasche based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Boris Pasche. Boris Pasche is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Choucair, Khalil, Md. Hafiz Uddin, Misako Nagasaka, et al.. (2025). Targeting KRAS mutations: orchestrating cancer evolution and therapeutic challenges. Signal Transduction and Targeted Therapy. 10(1). 385–385. 2 indexed citations
2.
Aboukameel, Amro, Husain Yar Khan, Md. Hafiz Uddin, et al.. (2024). RCC1 regulation of subcellular protein localization via Ran GTPase drives pancreatic ductal adenocarcinoma growth. Cancer Letters. 604. 217275–217275. 2 indexed citations
3.
Sohl, Stephanie J., Pamela W. Duncan, John M. Salsman, et al.. (2022). Adaptation of a Personalized Electronic Care Planning Tool for Cancer Follow-up Care: Formative Study. JMIR Formative Research. 7. e41354–e41354.
4.
Chang, Antao, Liang Liu, Dan Wu, et al.. (2021). Recruitment of KMT2C/MLL3 to DNA Damage Sites Mediates DNA Damage Responses and Regulates PARP Inhibitor Sensitivity in Cancer. Cancer Research. 81(12). 3358–3373. 39 indexed citations
5.
Jatoi, Aminah, Fang‐Shu Ou, Daniel H. Ahn, et al.. (2021). Preemptive Versus Reactive Topical Clobetasol for Regorafenib-Induced Hand-Foot Reactions: A Preplanned Analysis of the ReDOS Trial. The Oncologist. 26(7). 610–618. 5 indexed citations
6.
Gmeiner, William H., David L. Caudell, Ralph B. D’Agostino, et al.. (2020). Improved Antitumor Activity of the Fluoropyrimidine Polymer CF10 in Preclinical Colorectal Cancer Models through Distinct Mechanistic and Pharmacologic Properties. Molecular Cancer Therapeutics. 20(3). 553–563. 14 indexed citations
7.
Rimkus, Tadas, Richard L. Carpenter, Sherona Sirkisoon, et al.. (2018). Truncated Glioma-Associated Oncogene Homolog 1 (tGLI1) Mediates Mesenchymal Glioblastoma via Transcriptional Activation of CD44. Cancer Research. 78(10). 2589–2600. 32 indexed citations
8.
Xing, Fei, Yin Liu, Shih-Ying Wu, et al.. (2018). Loss of XIST in Breast Cancer Activates MSN-c-Met and Reprograms Microglia via Exosomal miRNA to Promote Brain Metastasis. Cancer Research. 78(15). 4316–4330. 259 indexed citations
9.
Xing, Fei, Yin Liu, Sambad Sharma, et al.. (2016). Activation of the c-Met Pathway Mobilizes an Inflammatory Network in the Brain Microenvironment to Promote Brain Metastasis of Breast Cancer. Cancer Research. 76(17). 4970–4980. 102 indexed citations
10.
Principe, Daniel R., Brian DeCant, Emman Mascariñas, et al.. (2016). TGFβ Signaling in the Pancreatic Tumor Microenvironment Promotes Fibrosis and Immune Evasion to Facilitate Tumorigenesis. Cancer Research. 76(9). 2525–2539. 156 indexed citations
11.
Costa, Frederico, et al.. (2012). Selecting patients for cytotoxic therapies in gastroenteropancreatic neuroendocrine tumours. Best Practice & Research Clinical Gastroenterology. 26(6). 843–854. 9 indexed citations
12.
Kaklamani, Virginia, Nengjun Yi, Kui Zhang, et al.. (2011). Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk. Metabolism. 60(9). 1234–1243. 47 indexed citations
13.
Zeng, Qinghua, Yanfei Xu, Maureen Sadim, et al.. (2009). Tgfbr1 Haploinsufficiency Is a Potent Modifier of Colorectal Cancer Development. Cancer Research. 69(2). 678–686. 45 indexed citations
14.
Strouch, Matthew J., Qinghua Zeng, Morgan R. Barron, et al.. (2009). Tgfbr1 Haploinsufficiency Inhibits the Development of Murine Mutant Kras -Induced Pancreatic Precancer. Cancer Research. 69(24). 9169–9174. 27 indexed citations
15.
Lei, Zhe, Rengyun Liu, Jun Zhao, et al.. (2009). TGFBR1 Haplotypes and Risk of Non–Small-Cell Lung Cancer. Cancer Research. 69(17). 7046–7052. 22 indexed citations
16.
Barbault, Alexandre, et al.. (2009). Amplitude-modulated electromagnetic fields for the treatment of cancer: Discovery of tumor-specific frequencies and assessment of a novel therapeutic approach. Journal of Experimental & Clinical Cancer Research. 28(1). 51–51. 109 indexed citations
17.
Valle, Laura, Sandya Liyanarachchi, Heather Hampel, et al.. (2008). Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer. Science. 321(5894). 1361–1365. 107 indexed citations
18.
Patel, Jyoti D., Boris Pasche, & Athanassios Argiris. (2004). Targeting non-small cell lung cancer with epidermal growth factor tyrosine kinase inhibitors: where do we stand, where do we go. Critical Reviews in Oncology/Hematology. 50(3). 175–186. 7 indexed citations
19.
Elgue, Graciela, Boris Pasche, Margareta Blombäck, & Per Olsson. (1990). The Use of a Commercial ELISA for Assay of Thrombin-Antithrombin Complexes in Purified Systems. Thrombosis and Haemostasis. 63(3). 435–438. 10 indexed citations
20.
Pasche, Boris, Koichi Kodama, Olle Larm, Per Olsson, & Jesper Swedenborg. (1986). Thrombin inactivation on surfaces with covalently bonded heparin. Thrombosis Research. 44(6). 739–748. 60 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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